Piperidine → HCID 67849436, compound

HRID 1197989Notes

Reaction equation

HRID 1197989 reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][C:3]=1[C:9](=[O:11])[CH3:10].[N:12]1[CH:17]=[CH:16][C:15]([C:18]([Cl:20])=O)=[CH:14][CH:13]=1.[NH:21]1[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]1>>[ClH:20].[N:21]1([CH2:6][CH2:7][CH2:2][CH2:3][CH2:4][CH2:5][O:8][C:5]2[CH:6]=[CH:7][C:2]3[O:1][C:18]([C:15]4[CH:16]=[CH:17][N:12]=[CH:13][CH:14]=4)=[CH:10][C:9](=[O:11])[C:3]=3[CH:4]=2)[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]1

Participants

4

Procedure

The compound was prepared by the method of Example 11 from 2',5'-dihydroxyacetophenone, 4-pyridylcarbonyl chloride, and piperidine: mp 186°-187 ° C.

Sources & evidence

ORD record
ord-5f4196cc808941a68af6ed1e52a59040
Source dataset
uspto-grants-1994_01
Patent number
US05278174

Reaction notes

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